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Subcapsular sinus macrophages in lymph nodes clear lymph-borne viruses and present them to antiviral B cells
Abstract
Lymph nodes prevent the systemic dissemination of pathogens such as viruses that infect peripheral tissues after penetrating the body's surface barriers. They are also the staging ground of adaptive immune responses to pathogen-derived antigens. It is unclear how virus particles are cleared from afferent lymph and presented to cognate B cells to induce antibody responses. Here we identify a population of CD11b+CD169+MHCII+ macrophages on the floor of the subcapsular sinus (SCS) and in the medulla of lymph nodes that capture viral particles within minutes after subcutaneous injection. Macrophages in the SCS translocated surface-bound viral particles across the SCS floor and presented them to migrating B cells in the underlying follicles. Selective depletion of these macrophages compromised local viral retention, exacerbated viraemia of the host, and impaired local B-cell activation. These findings indicate that CD169+ macrophages have a dual physiological function. They act as innate 'flypaper' by preventing the systemic spread of lymph-borne pathogens and as critical gatekeepers at the lymph-tissue interface that facilitate the recognition of particulate antigens by B cells and initiate humoral immune responses.
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“These macrophages can capture larger molecules, viruses, and bacteria (89, 90) and are capable of mounting a protective immune response even in the absence of antigen-presenting DCs (91).”
From Transport and Immune Functions of the Lymphatic System. (2025) · cites this paper as [90]
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Cites
T-cell priming by dendritic cells in lymph nodes occurs in three distinct phases
Mempel, T. R., Henrickson, S. E., & von Andrian, U. H. (2004) · Nature · doi:10.1038/nature02238 · Cited by 1,720
Self-citationMACROPHAGE RECEPTORS AND IMMUNE RECOGNITION
Taylor, P. R., Martínez‐Pomares, L., Stacey, M. A., Lin, H.-H., Brown, G. D., & Gordon, S. (2005) · Annual Review of Immunology · doi:10.1146/annurev.immunol.23.021704.115816 · Cited by 1,366
Homing and cellular traffic in lymph nodes
von Andrian, U. H., & Mempel, T. R. (2003) · Nature reviews. Immunology · doi:10.1038/nri1222 · Cited by 1,271
Self-citationCD69 acts downstream of interferon-α/β to inhibit S1P1 and lymphocyte egress from lymphoid organs
Shiow, L. R., Rosen, D. B., Brdičková, N., Xu, Y., An, J., Lanier, L. L., Cyster, J. G., & Matloubian, M. (2006) · Nature · doi:10.1038/nature04606 · Cited by 1,189
Control of Early Viral and Bacterial Distribution and Disease by Natural Antibodies
Ochsenbein, A. F., Fehr, T. H., Lutz, C., Suter, M., Brombacher, F., Hengartner, H., & Zinkernagel, R. M. (1999) · Science · doi:10.1126/science.286.5447.2156 · Cited by 911
Okada, T., Miller, M. J., Parker, I., Krummel, M. F., Neighbors, M., Hartley, S. B., O’Garra, A., Cahalan, M. D., & Cyster, J. G. (2005) · PLoS Biology · doi:10.1371/journal.pbio.0030150 · Cited by 586
Balanced responsiveness to chemoattractants from adjacent zones determines B-cell position
Reif, K., Ekland, E. H., Ohl, L., Nakano, H., Lipp, M., Förster, R., & Cyster, J. G. (2002) · Nature · doi:10.1038/416094a · Cited by 572
B cell receptor signal strength determines B cell fate
Casola, S. S., Otipoby, K. L., Alimzhanov, M. B., Humme, S., Uyttersprot, N., Kutok, J. L., Carroll, M. C., & Rajewsky, K. (2004) · Nature Immunology · doi:10.1038/ni1036 · Cited by 561
Extrafollicular Activation of Lymph Node B Cells by Antigen-Bearing Dendritic Cells
Qi, H., Egen, J. G., Huang, A. Y.-C., & Germain, R. N. (2006) · Science · doi:10.1126/science.1125703 · Cited by 521
Wessels, M. R., Butko, P., Ma, M., Warren, H. B., Lage, A. L., & Carroll, M. C. (1995) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.92.25.11490 · Cited by 503
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Wiig, H., Keskin, D., & Kalluri, R. (2010) · Matrix Biology · doi:10.1016/j.matbio.2010.08.001 · Cited by 87
Model of colonic inflammation: Immune modulatory mechanisms in inflammatory bowel disease
Wendelsdorf, K. V., Bassaganya-Riera, J., Hontecillas, R., & Eubank, S. (2010) · Journal of Theoretical Biology · doi:10.1016/j.jtbi.2010.03.027 · Cited by 90
Ganchua, S. K. C., Cadena, A. M., Maiello, P. A., Gideon, H. P., Myers, A. J., Junecko, B. A. F., Klein, E. C., Lin, P. L., Mattila, J. T., & Flynn, J. L. (2018) · PLoS Pathogens · doi:10.1371/journal.ppat.1007337 · Cited by 90
Hamel, K. M., Liarski, V. M., & Clark, M. R. (2012) · Autoimmunity · doi:10.3109/08916934.2012.665524 · Cited by 92
Sialoadhesin in recognition of self and non-self
Klaas, M., & Crocker, P. R. (2012) · Seminars in Immunopathology · doi:10.1007/s00281-012-0310-3 · Cited by 86
Location, location, location: tissue-specific regulation of immune responses
Hu, W., & Pasare, C. (2013) · Journal of Leukocyte Biology · doi:10.1189/jlb.0413207 · Cited by 92
The Cytoskeleton Coordinates the Early Events of B-cell ActivationPreprint
Harwood, N. E., & Batista, F. D. (2010) · Cold Spring Harbor Perspectives in Biology · doi:10.1101/cshperspect.a002360 · Cited by 89
Hickman, H. D., Reynoso, G. V., Ngudiankama, B. F., Rubin, E. J., Magadán, J. G., Cush, S. S., Gibbs, J. S., Molon, B., Bronte, V., Bennink, J. R., et al. (2013) · Cell Host & Microbe · doi:10.1016/j.chom.2013.01.004 · Cited by 84
Implications of Lymphatic Transport to Lymph Nodes in Immunity and Immunotherapy
Thomas, S. N., Rohner, N. A., & Edwards, E. E. (2016) · Annual Review of Biomedical Engineering · doi:10.1146/annurev-bioeng-101515-014413 · Cited by 87
Functions of CD169 positive macrophages in human diseases (Review)
Liu, Y., Yuan, X., & Qiu, C. (2020) · Biomedical Reports · doi:10.3892/br.2020.1402 · Cited by 90
Purtha, W. E., Chachu, K. A., Virgin, H. W., & Diamond, M. (2008) · Journal of Virology · doi:10.1128/jvi.01646-08 · Cited by 84
Ligand Mobility Regulates B Cell Receptor Clustering and Signaling Activation
Ketchum, C. M., Miller, H. E., Song, W., & Upadhyaya, A. (2014) · Biophysical Journal · doi:10.1016/j.bpj.2013.10.043 · Cited by 80
The role of lymph node sinus macrophages in host defense
Kuka, M., & Iannacone, M. (2014) · Annals of the New York Academy of Sciences · doi:10.1111/nyas.12387 · Cited by 80
Self-citationDelivery of nanovaccine towards lymphoid organs: recent strategies in enhancing cancer immunotherapy
Cai, T., Liu, H., Zhang, S., Hu, J. Y., & Zhang, L. L. (2021) · Journal of Nanobiotechnology · doi:10.1186/s12951-021-01146-2 · Cited by 79
Lymph node macrophages: Scavengers, immune sentinels and trophic effectors
Bellomo, A., Gentek, R., Bajénoff, M., & Baratin, M. (2018) · Cellular Immunology · doi:10.1016/j.cellimm.2018.01.010 · Cited by 82
Espéli, M., Smith, K. G. C., & Clatworthy, M. R. (2015) · Immunological Reviews · doi:10.1111/imr.12368 · Cited by 79
Shinde, P. V., Xu, H. C., Maney, S. K., Kloetgen, A., Namineni, S., Zhuang, Y., Honke, N., Shaabani, N., Bellora, N., Doerrenberg, M., et al. (2017) · Journal of Virology · doi:10.1128/jvi.01637-17 · Cited by 76
Self-citationLipid-Mediated Targeting with Membrane-Wrapped Nanoparticles in the Presence of Corona Formation
Xu, F., Reiser, M. L., Yu, X., Gummuluru, S., Wetzler, L. M., & Reinhard, B. M. (2015) · ACS Nano · doi:10.1021/acsnano.5b06501 · Cited by 78
Klaas, M., Oetke, C., Lewis, L. E., Erwig, L. P., Heikema, A. P., Easton, A., Willison, H. J., & Crocker, P. R. (2012) · The Journal of Immunology · doi:10.4049/jimmunol.1200776 · Cited by 75
Designing CD8+ T cell vaccines: it's not rocket science (yet)
Yewdell, J. W. (2010) · Current Opinion in Immunology · doi:10.1016/j.coi.2010.04.002 · Cited by 77
Fang, V., Chaluvadi, V. S., Ramos-Pérez, W. D., Mendoza, A., Baeyens, A., Rivera, R. R., Chun, J. J. M., Cammer, M., & Schwab, S. R. (2016) · Nature Immunology · doi:10.1038/ni.3619 · Cited by 78
Recording the wild lives of immune cells
Pittet, M. J., Garris, C., Arlauckas, S. P., & Weissleder, R. (2018) · Science Immunology · doi:10.1126/sciimmunol.aaq0491 · Cited by 75
Magnusson, S. E., Altenburg, A. F., Bengtsson, K. L., Bosman, F., de Vries, R. D., Rimmelzwaan, G. F., & Stertman, L. (2018) · Immunologic Research · doi:10.1007/s12026-018-8991-x · Cited by 74
Regulation of integrin activation through the B-cell receptor
Arana, E., Harwood, N. E., & Batista, F. D. (2008) · Journal of Cell Science · doi:10.1242/jcs.017905 · Cited by 75
Perez‐Shibayama, C., Islander, U., Lütge, M., Cheng, H., Onder, L., Ring, S. S., Martin, A. D., Novković, M., Colston, J., Gil‐Cruz, C., et al. (2020) · Science Immunology · doi:10.1126/sciimmunol.abb7066 · Cited by 73
Molecular basis for potent B cell responses to antigen displayed on particles of viral size
Brooks, J. F., Riggs, J. B., Mueller, J. L., Mathenge, R., Wholey, W.-Y., Meyer, A. R., Yoda, S.-T., Vykunta, V. S., Nielsen, H. V., Cheng, W., et al. (2023) · Nature Immunology · doi:10.1038/s41590-023-01597-9 · Cited by 74
Lymphoid stroma in the initiation and control of immune responses
Mueller, S. N., & Ahmed, R. (2008) · Immunological Reviews · doi:10.1111/j.1600-065x.2008.00657.x · Cited by 73
Garcia, Z., Lemaı̂tre, F., van Rooijen, N., Albert, M. L., Lévy, Y., Schwartz, O., & Bousso, P. (2012) · Blood · doi:10.1182/blood-2012-02-408179 · Cited by 71
Allie, S. R., & Randall, T. D. (2020) · Viral Immunology · doi:10.1089/vim.2019.0141 · Cited by 73
Transcriptional and Metabolic Control of Memory B Cells and Plasma Cells
Ripperger, T. J., & Bhattacharya, D. (2021) · Annual Review of Immunology · doi:10.1146/annurev-immunol-093019-125603 · Cited by 72
The Mammalian Response to Virus Infection Is Independent of Small RNA Silencing
Backes, S., Langlois, R. A., Schmid, S., Varble, A., Shim, J. V., Sachs, D. M., & tenOever, B. R. (2014) · Cell Reports · doi:10.1016/j.celrep.2014.05.038 · Cited by 70
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Farrell, H. E., Davis-Poynter, N. J., Bruce, K. L., Lawler, C., Dölken, L., Mach, M., & Stevenson, P. G. (2015) · Journal of Virology · doi:10.1128/jvi.00480-15 · Cited by 72
The microanatomy of B cell activation
Phan, T. G., Gray, E. E., & Cyster, J. G. (2009) · Current Opinion in Immunology · doi:10.1016/j.coi.2009.05.006 · Cited by 75
Fink, K., Ng, C., Nkenfou, C. N., Vasudevan, S. G., van Rooijen, N., & Schul, W. (2009) · European Journal of Immunology · doi:10.1002/eji.200939389 · Cited by 72
Self-citationLoo, C. P., Nelson, N. A., Lane, R. S., Booth, J. L., Hardin, S. C. L., Thomas, A., Slifka, M. K., Nolz, J. C., & Lund, A. W. (2017) · Cell Reports · doi:10.1016/j.celrep.2017.09.006 · Cited by 71
Mystery eye: Human adenovirus and the enigma of epidemic keratoconjunctivitis
Jonas, R. A., Ung, L., Rajaiya, J., & Chodosh, J. (2019) · Progress in Retinal and Eye Research · doi:10.1016/j.preteyeres.2019.100826 · Cited by 69
Adding new dimensions: towards an integrative understanding of HIV-1 spread
Fackler, O., Murooka, T. T., Imle, A., & Mempel, T. R. (2014) · Nature Reviews Microbiology · doi:10.1038/nrmicro3309 · Cited by 73
Self-citationThe molecular assembly and organization of signaling active B‐cell receptor oligomers
Tolar, P., Sohn, H. W., Liu, W., & Pierce, S. K. (2009) · Immunological Reviews · doi:10.1111/j.1600-065x.2009.00833.x · Cited by 71
Antigen-Induced Oligomerization of the B Cell Receptor Is an Early Target of FcγRIIB Inhibition
Liu, W., Sohn, H. W., Tolar, P., Meckel, T., & Pierce, S. K. (2010) · The Journal of Immunology · doi:10.4049/jimmunol.0902334 · Cited by 68
Galea, R. C., Nel, H. J., Talekar, M., Liu, X., Ooi, J. D., Huynh, M., Hadjigol, S., Robson, K. J., Ting, Y. T., Cole, S., et al. (2019) · JCI Insight · doi:10.1172/jci.insight.126025 · Cited by 68
Martin, J. T., Cottrell, C. A., Antanasijevic, A., Carnathan, D. G., Cossette, B. J., Enemuo, C. A., Gebru, E. H., Choe, Y., Viviano, F., Fischinger, S., et al. (2020) · npj Vaccines · doi:10.1038/s41541-020-00223-1 · Cited by 67
CD169+ macrophage intrinsic IL-10 production regulates immune homeostasis during sepsis
Yeung, S. T., Ovando, L., Russo, A. J., Rathinam, V. A. K., & Khanna, K. M. (2023) · Cell Reports · doi:10.1016/j.celrep.2023.112171 · Cited by 68
Komohara, Y., Ohnishi, K., & Takeya, M. (2016) · Cancer Science · doi:10.1111/cas.13137 · Cited by 70
Xu, R.-H., Wong, E. B., Rubio, D., Roscoe, F., Ma, X., Nair, S., Remakus, S., Schwendener, R. A., John, S. A., Shlomchik, M. J., et al. (2015) · Immunity · doi:10.1016/j.immuni.2015.11.015 · Cited by 67
CD169+ lymph node macrophages have protective functions in mouse breast cancer metastasis
Tacconi, C., Commerford, C. D., Dieterich, L. C., Schwager, S., He, Y., Ikenberg, K., Friebel, E., Becher, B., Tugues, S., & Detmar, M. J. (2021) · Cell Reports · doi:10.1016/j.celrep.2021.108993 · Cited by 65
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Hirosue, S., & Dubrot, J. (2015) · Frontiers in Immunology · doi:10.3389/fimmu.2015.00446 · Cited by 70
Liu, C., Miller, H. E., Orlowski, G. M., Hang, H., Upadhyaya, A., & Song, W. (2012) · The Journal of Immunology · doi:10.4049/jimmunol.1103065 · Cited by 71
Veninga, H., Borg, E. G. F., Vreeman, K., Taylor, P. R., Kalay, H., van Kooyk, Y., Kraal, G., Martínez‐Pomares, L., & den Haan, J. M. M. (2014) · European Journal of Immunology · doi:10.1002/eji.201444983 · Cited by 63
Fischer, M. A., Davies, M. L., Reider, I. E., Heipertz, E. L., Epler, M., Sei, J. J., Ingersoll, M. A., van Rooijen, N., Randolph, G. J., & Norbury, C. C. (2011) · PLoS Pathogens · doi:10.1371/journal.ppat.1002374 · Cited by 63
Coombes, J. L., Han, S., van Rooijen, N., Raulet, D. H., & Robey, E. A. (2012) · Cell Reports · doi:10.1016/j.celrep.2012.06.001 · Cited by 64
Bravo‐Blas, A., Utriainen, L., Clay, S. L., Kästele, V., Cerovic, V., Cunningham, A. F., Henderson, I. R., Wall, D. M., & Milling, S. W. F. (2018) · The Journal of Immunology · doi:10.4049/jimmunol.1701254 · Cited by 63
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Xu, R.-H., Remakus, S., Ma, X., Roscoe, F., & Sigal, L. J. (2010) · PLoS Pathogens · doi:10.1371/journal.ppat.1000768 · Cited by 62
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Myelin-phagocytosing macrophages modulate autoreactive T cell proliferation
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Khairnar, V., Duhan, V., Maney, S. K., Honke, N., Shaabani, N., Pandyra, A. A., Seifert, M., Pozdeev, V. I., Xu, H. C., Sharma, P., et al. (2015) · Nature Communications · doi:10.1038/ncomms7217 · Cited by 59
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Bošnjak, B., Do, K. T. H., Förster, R., & Hammerschmidt, S. I. (2021) · Immunological Reviews · doi:10.1111/imr.13050 · Cited by 59
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Gaspar, M. A., May, J. S., Sukla, S., Frederico, B., Gill, M. B., Smith, C. M., Belz, G. T., & Stevenson, P. G. (2011) · PLoS Pathogens · doi:10.1371/journal.ppat.1002346 · Cited by 57
Edgar, L. J., Kawasaki, N., Nycholat, C. M., & Paulson, J. C. (2018) · Cell chemical biology · doi:10.1016/j.chembiol.2018.10.006 · Cited by 57
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Zhang, Y.-N., Poon, W., Sefton, E., & Chan, W. C. W. (2020) · ACS Nano · doi:10.1021/acsnano.0c02240 · Cited by 55
Willis, E., Pardi, N., Parkhouse, K., Mui, B. L., Tam, Y. K., Weissman, D., & Hensley, S. E. (2020) · Science Translational Medicine · doi:10.1126/scitranslmed.aav5701 · Cited by 54
Innate and adaptive immune responses toward nanomedicines
Viana, I. M. D. O., Roussel, S., Defrêne, J., Lima, E. M., Barabé, F., & Bertrand, N. (2021) · Acta Pharmaceutica Sinica B · doi:10.1016/j.apsb.2021.02.022 · Cited by 57
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Akiyama, H., Ramirez, N.-G. P., Gibson, G. A., Kline, C. E., Watkins, S. C., Ambrose, Z., & Gummuluru, S. (2017) · Journal of Virology · doi:10.1128/jvi.00972-17 · Cited by 55
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Zhang, X., Zhao, Q., Wen, L., Wu, C., Yao, Z., Yan, Z., Li, R., Chen, L., Chen, F., Xie, Z., et al. (2021) · Frontiers in Veterinary Science · doi:10.3389/fvets.2021.688611 · Cited by 53
Depoil, D., Weber, M., Treanor, B., Fleire, S. J., Carrasco, Y. R., Harwood, N. E., & Batista, F. D. (2009) · Science Signaling · doi:10.1126/scisignal.263pt1 · Cited by 58
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Frederico, B., Milho, R., May, J. S., Gillet, L., & Stevenson, P. G. (2012) · PLoS Pathogens · doi:10.1371/journal.ppat.1002935 · Cited by 53
Phan, T. G., & Tangye, S. G. (2017) · Current Opinion in Immunology · doi:10.1016/j.coi.2017.03.005 · Cited by 55
Visualizing a role for the actin cytoskeleton in the regulation of B‐cell activation
Batista, F. D., Treanor, B., & Harwood, N. E. (2010) · Immunological Reviews · doi:10.1111/j.1600-065x.2010.00943.x · Cited by 52
Beier, K. T., Saunders, A. B., Oldenburg, I. A., Sabatini, B. L., & Cepko, C. L. (2013) · Frontiers in Neural Circuits · doi:10.3389/fncir.2013.00011 · Cited by 52
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Self-citationXu, Y., Xu, L., Zhao, M., Xu, C., Fan, Y., Pierce, S. K., & Liu, W. (2014) · Cell Research · doi:10.1038/cr.2014.65 · Cited by 50
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Chen, Q., Qi, C., Peng, G., Liu, Y., Zhang, X., & Meng, Z. (2018) · Food and Agricultural Immunology · doi:10.1080/09540105.2018.1461198 · Cited by 49
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Metadata
- Authors
- Junt, T., Moseman, E. A., Iannacone, M., Massberg, S., Lang, P. A., Boes, M., Fink, K., Henrickson, S. E., Shayakhmetov, D. M., Di Paolo, N. C., van Rooijen, N., Mempel, T. R., Whelan, S. P., & von Andrian, U. H.
- Affiliations
- Harvard University (US)
- University Hospital Zurich (CH)
- Brigham and Women's Hospital (US)
- Novartis Institute For Tropical Diseases (SG)
- University of Washington (US)
- Vrije Universiteit Amsterdam (NL)
- Corresponding author
- von Andrian, Ulrich H.
- ORCID
- Venue
- Nature
- Published
- 2007-10-14
- Volume
- 450
- Issue
- 7166
- Pages
- 110-114
- ISSN
- 0028-0836 (ISSN-L)
- 1476-4687
- OpenAlex
- W2019206924
- Cited by
- 846
- References
- 29
- Citations by year
- 2026: 21 · 2025: 38 · 2024: 37 · 2023: 34 · 2022: 35 · 2021: 55 · 2020: 46 · 2019: 49 · 2018: 53 · 2017: 53 · 2016: 46 · 2015: 53 · 2014: 46 · 2013: 38 · 2012: 66
- FWCI
- 17.12
- Type
- journal article
- Language
- en
- Open access
- closed
- Licence
- Locations
- Nature (publishedVersion)
- PubMed (publishedVersion)
- RePEc: Research Papers in Economics (submittedVersion)
- Archivio Istituzionale della Ricerca - Università Vita-Salute San Raffaele (submittedVersion)
- mediaTUM (Technical University of Munich) (submittedVersion)
- Funders
- National Institute of General Medical Sciences (T32GM007753)
- National Institute of Allergy and Infectious Diseases (R01AI059371)
- Topics
- Life Sciences › Immunology and Microbiology › Immunology › Immunotherapy and Immune Responses
- Life Sciences › Immunology and Microbiology › Immunology › T-cell and B-cell Immunology
- Life Sciences › Immunology and Microbiology › Immunology › Immune responses and vaccinations
- Keywords
- subcapsular sinus macrophages, lymph node macrophages, CD169+ macrophages, viral clearance, B cell activation, antigen presentation, afferent lymph, humoral immune response, viremia, macrophage depletion
- MeSH terms
- Animals, Antibody Formation, B-Lymphocytes, Cell Line, Lymph, Lymph Nodes, Macrophages, Membrane Glycoproteins, Mice, Inbred C57BL, Receptors, Immunologic, Vesiculovirus, CD11b Antigen, Mice, Sialic Acid Binding Ig-like Lectin 1
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